Calazel P, Martinez J
Arch Mal Coeur Vaiss. 1975 Apr;68(4):397-403.
In relation with 4 cases of anomalous branching of one pulmonary artery from the ascending aorta, the main clinical, angiographic, physiopathologic, therapeutic and embryologic features of this malformation were reviewed. It appeared that the natural history of this malformation is a severe one, and only a corrective surgical treatment is liable to secure survival and cure. This anomaly was also encountered, very rarely, in Fallot's tetralogy, and two cases of this combination were reported.
针对4例肺动脉从升主动脉异常分支的病例，回顾了这种畸形的主要临床、血管造影、生理病理、治疗及胚胎学特征。结果显示，这种畸形的自然病程较为严重，只有通过矫正性外科治疗才有望确保存活和治愈。在法洛四联症中也极罕见地遇到这种异常情况，本文报告了2例这种联合病例。
